US20060111515A1

US20060111515A1 - Clear, impact modified, heat resistant polyvinyl halide compositions

Info

Publication number: US20060111515A1
Application number: US10/995,605
Authority: US
Inventors: Larry Simmons; George McCarty
Original assignee: Chemtura Corp
Current assignee: Galata Chemicals LLC
Priority date: 2004-11-22
Filing date: 2004-11-22
Publication date: 2006-05-25
Also published as: AR052983A1; US7723433B2; CN1810876B; WO2006057827A1; TW200632022A; US20100197860A1; CN1810876A

Abstract

A clear, impact modified, heat resistant polyvinyl chloride composition is provided comprising (a) at least one polyvinyl halide; (b) at least one clear impact modifier possessing a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide; and (c) at least one clear heat modifier comprising a terpolymer obtained by the copolymerization of a vinyl aromatic monomer, an acrylonitrile and an alkyl acrylate or alkyl methacrylate, wherein the terpolymer possesses a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide and possesses a weight average molecular weight ranging from about 75,000 to about 400,000.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention
This invention relates to polyvinyl halide compositions that possess dimensional stability to heat, impact strength and clarity. More particularly, the invention relates to a polyvinyl halide composition which is excellent in optical properties, impact resistance and heat resistance and can be employed in a wide variety of applications such as films, sheets, pipes, cable ducts, deck plates, building materials, battery housings, and industrial components.
2. Description of the Related Art
Polyvinyl chloride resins (PVC) are well known thermoplastic resins that can be compounded with a variety of property enhancing additives and molded, extruded, calendered or formed for a variety of applications. The art of PVC compounding is extremely complex in that many ingredients interact with each other. This complexity means that levels of ingredients and types of ingredients must be varied to yield a PVC compound that is useful for a given application.
Articles such as bottles, packages and films for certain markets demand a high degree of clarity. A property of PVC that is important for many applications is its inherent clarity and transparency. However, PVC resins are generally quite brittle. To overcome this deficiency, rubbery impact modifiers having glass transition temperatures below that of PVC are incorporated into the resin. Impact modifiers based on graft copolymers prepared by conventional radical polymerization are well known and have been widely employed for over thirty years. Graft copolymers of styrene, α-methylstyrene, acrylonitrile, methacrylic acid esters or mixtures thereof on a rubber, e.g., polybutadiene or a butadiene copolymer, and mixtures of such graft polymers with polystyrene or styrene copolymers are well known PVC impact modifiers. A variety of clear PVC impact modifiers are now commercially available. These impact modifiers possess refractive indices that closely match that of PVC in order to preserve the clarity and transparency of the PVC resin.
The freezing temperature (glass transition temperature) of PVC is about 80° C. so that its dimensional stability to heat (Vicat temperatures of about 75° to 84° C.) is insufficient for many applications where prolonged exposure to heat is encountered. Attempts have been made to improve the dimensional stability (heat resistance) of PVC by modifying the molecular structure of PVC, carrying out chemical after-treatments or adding thermoplastic resins with higher glass transition temperatures to the PVC base resin. Typical heat distortion temperature (HDT) modifiers can be used to raise HDT, but the result is an opaque compound that does not allow for use in PVC compounds where clarity is required. Known HDT modifiers that are opaque include acrylonitrile-α methylstyrene copolymer, acrylonitrile-α methylstyrene-butadiene copolymer and polymethyl methacrylate-acrylic ester copolymer (PMMA).
U.S. Pat. No. 5,166,271 discloses a heat resistant PVC copolymer obtained by graft copolymerizing a vinyl chloride resin with N-substituted maleimide in the presence of a radical polymerizable monomer which (1) is liquid at the temperature of copolymerization, (2) is capable of dissolving the N-substituted maleimide and (3) has a glass transition temperature of the polymer of 70° C. or more.
U.S. Pat. No. 5,206,296 discloses a processing aid for polymeric compositions such as PVC comprising a high molecular weight terpolymer comprising 10-49% by weight of a vinyl aromatic monomer such as styrene, 5-35% by weight of acrylonitrile, and 21-60% of an alkyl acrylate or alkyl methacrylate. The terpolymer disclosed in U.S. Pat. No. 5,206,296 possesses a viscosity of more than four as measured in dimethylformamide as 30° C. at a concentration of 100 mg terpolymer per 100 ml dimethylformamide. The average molecular weights of the terpolymer processing aid exceed 2,000,000, and are used at levels of 0.1 to 20 parts by weight per 100 parts by weight of PVC.
U.S. Pat. No. 5,354,812 discloses ternary alloys of PVC, post-chlorinated PVC (CPVC), and alloying polymers wherein the alloying polymers enhance the heat distortion temperature of the CPVC.
A combination of clear impact modifier and clear heat modifier that provides improved PVC compositions characterized by their clarity (light transmission), heat distortion temperature, and impact strength would be a useful advance in the PVC compounding art.

SUMMARY OF THE INVENTION

It is an object of the invention to provide a clear, impact modified, heat resistant polyvinyl halide composition. In one embodiment, the polyvinyl halide composition comprises
(a) at least one polyvinyl halide;
(b) at least one clear impact modifier possessing a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide; and
(c) at least one clear heat modifier comprising a terpolymer obtained by the copolymerization of a vinyl aromatic monomer, an acrylic nitrile and an alkyl acrylate or alkyl methacrylate, wherein the terpolymer possesses a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide and possesses a weight average molecular weight ranging from about 75,000 to about 400,000; and
wherein (a) comprises from about 20 to about 50 weight percent, (b) comprises from about 10 to about 30 weight percent, and (c) comprises from about 20 to about 80 weight percent, based on the combined weight of (a), (b) and (c).

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Clear, impact modified and heat modified polyvinyl halide compositions of the present invention can be prepared by conventional means such as, for example, melt-compounding a mixture of polyvinyl halide resin, clear impact modifier possessing a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide, and clear heat modifier comprising a terpolymer obtained by the copolymerization of a vinyl aromatic monomer, an acrylic nitrile and an alkyl acrylate or alkyl methacrylate, wherein the terpolymer possesses a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl chloride and possesses a weight average molecular weight ranging from about 75,000 to about 400,000.
The polyvinyl halide resins that are employed in the clear thermoplastic resin compositions of this invention include, for example, vinyl halide homopolymers, vinyl halide copolymers and polymer blends containing vinyl halide homopolymer or copolymers. Examples of vinyl halide homopolymers, include, but are not limited to, polyvinyl chloride, polyvinylidiene chloride, polyvinyl bromide, polyvinyl fluoride, and polyvinylidene fluoride. Examples of ethylenically unsaturated monomers which can be copolymerized with vinyl chloride include, but are not limited to, vinylidene chloride, vinyl acetate, vinyl butyrate, vinyl benzoate, diethyl fumarate, diethyl maleate, other alkyl fumarates and maleates, vinyl propionate methyl acrylate, 2-ethylhexyl acrylate, butyl acryalate, ethyl acrylate, and other alkyl acrylates, methyl methacrylate, ethyl methacrylate, butyl methacrylate, hydroxyethyl methacrylate and other alkyl methacrylates, methyl alpha chloracrylate, styrene, vinyl ethers such as vinyl ethyl ether, vinyl chloroethyl ether, vinyl phenyl ether, vinyl ketones such as vinyl methyl ketone, vinyl phenyl ketone, 1-fluoro-1-chloroethylene, acrylonitrile, chloroacrylonitrile, allylidene diacetate, chloroallylidene diacetate, ethylene and propylene. Examples of polymer blends include, but are not limited to blends of polyvinyl chloride and polyethylene, polyvinyl chloride and chlorinated polyethylene, polyvinyl chloride and polymethyl methacrylate, polyvinyl chloride and polybutylmethacrylate, polyvinyl chloride and polystyrene, polyvinyl chloride and acrylonitrile-butadiene-styrene copolymer, and polyvinyl chloride and polyethylene and polymethyl methacrylate.
The polymer blends usable in the practice of this invention can include physical blends of at least two distinct polymeric species and contain from about 25 to about 95 weight percent of vinyl halide homopolymer.
The term “impact modifier” in the context of this invention refers to rubber and rubber modified with a thermoplastic resin, which furthermore possesses a refractive index that is within plus or minus 2% of the refractive index of the polyvinyl halide resin, preferably a refractive index of not more than about 1% above or below the refractive index of the polyvinyl halide, and more preferably a refractive index which is not more than about 0.05% above or below the refractive index of the polyvinyl halide. Such impact modifiers are well known in the art.
The terpolymer of the clear heat modifier for use in the compostion of the present invention includes from about 30 to about 50 and preferably from about 35 to about 45% by weight of the vinyl aromatic monomers, from about 15 to about 35 and preferably from about 20 to about 30% by weight of the acrylic nitrile and from about 25 to about 45 and preferably from about 30 to about 40% by weight of the alkyl acrylate or alkyl methacrylate, based on the total weight of the terpolymer.
Suitable vinyl aromatic monomers include, but are not limited to, styrene, alpha methylstyrene, halogenated styrene, vinyltoluene, alkoxystyrene and other styrene derivatives that are copolymerizable with an acrylic nitrile and an alkyl methacrylate and the like and mixtures thereof.
Suitable acrylic nitrile monomers include, but are not limited to, methacrylonitrile, ethacrylonitrile, chloroacrylonitrile, acrylonitrile, and the like and mixtures thereof.
Suitable alkyl acrylates and alkyl methacrylates include, but are not limited to, methyl acrylate, ethyl acrylate and the corresponding methacrylates and the like and mixtures thereof.
Polymerization of the monomers can be carried out in accordance with well known polymerization procedures known to those skilled in the art. An important feature of the invention is the low average molecular weight of the terpolymer that, in turn, permits the use of much higher loadings of the heat modifier in the PVC resin compared to higher molecular weight HDT resins. The weight average molecular weight of the terpolymer will range from about 75,000 to about 400,000, and preferably from about 100,000 to about 200,000. The resulting terpolymer will also possess a refractive index that is within plus or minus 2% of the refractive index of the polyvinyl halide resin, preferably a refractive index of not more than about 1% above or below the refractive index of the polyvinyl halide, and more preferably a refractive index which is not more than about 0.05% above or below the refractive index of the polyvinyl halide.
The amount of polyvinyl halide resin can range from about 10 to about 80 weight percent, and preferably from about 20 to about 50 weight percent, based on the combined weight of polyvinyl halide resin, clear impact modifier and clear heat modifier. The clear impact modifier is employed at a loading of from about 0 to about 35 weight percent, preferably from about 10 to about 25 weight percent, based on the combined weight of polyvinyl halide resin, clear impact modifier and clear heat modifier. The clear heat modifier is employed in an amount of from about 20 to about 80 weight percent, preferably from about 30 to about 60 weight percent based on the combined weight of polyvinyl halide resin, clear impact modifier and clear heat modifier.
Accordingly, the polyvinyl halide compositions of the present invention can have the capacity to be impact-modified to achieve notched Izod values generally in excess of 100 N·m/m (of notch), desirably in excess of 200 N·m/m, and preferably in excess of 230 N·m/m. Illustrative impact modifiers include, but are not limited to, ethylene-vinyl acetate copolymer (EVA), ethylene-propylene copolymer (EPR), polybutadiene-acrylonitrile-styrene copolymer (ABS), polybutylacrylate-acrylonitrile-styrene copolymer (ASA), polybutadiene-styrene-methyl methacrylate (MBS), polybutylacrylate, crosslinked acrylic rubber, styrene-butadiene copolymer (SBR) and acrylonitrile-butadiene copolymer (NBR).
In one embodiment, a process for preparing a clear, impact modified, heat resistant polyvinyl chloride composition includes the steps of combining components (a), (b) and (c) of the above-identified polyvinyl chloride composition in any known manner.
If desired, the composition may further include conventional additives such as, for example, heat stabilizers, antioxidants, lubricants, toners, colorants, dyes, and the like as is commonly practiced in the art of compounding clear impact modified polyvinyl halide resins. Compounding may be accomplished by conventional means, including Banbury mixers, heated roll mills, compounding extruders, and the like. Alternatively, for many applications the components will be mixed in powdered form, using any of a variety of high intensity mixers, to provide a dry powdered composition which will then be fabricated by methods such as calendering, milling, blow molding, and the like.
The practice of this invention will be better understood by consideration of the following Examples. All parts given are by weight unless otherwise indicated. Transparency refers to the transmitted intensity for all light that deviates by an angle θ>25°, as a percentage of the incident-light intensity. Haze refers to the integrated, transmitted intensity for all light that deviates by an angle θ<25°, as percentage of the incident-light intensity. Impact strengths are reported as ⅛″ notched Izod (NI) according to ASTM D256-2002 at 25° C. unless otherwise specified. Yellowing is measured by yellowness index (YI). These Examples are provided by way of illustration of the invention and are not intended to be limiting.

EXAMPLES 1-20 AND COMPARATIVE EXAMPLE A

The following components set forth in Table 1 were compounded to form PVC compositions in accordance with the present invention:

TABLE 1


Component	Composition

PVC K60 (614)	Polyvinyl chloride resin available from
	Formosa . . . R.I. = ˜1.54 available from
	Formosa Corp.
PVC K66	Polyvinyl chloride resin available from Polyone
(110 × 427)	R.I. = ˜1.54 available from Formosa Corp.
HDT Modifier	Terpolymer comprising 20-60% styrene, 10-40%
	acrylonitrile and 15-55% methyl methacrylate,
	R.I. = ˜1.53-1.55, M.W. = 75,000-400,000 available
	from Crompton Corporation, Middlebury, CT
B336	Blendex 336 Impact Modifier available from
	Crompton Corporation, Middlebury, CT comprising
	Acrylonitrile-polybutadiene-styrene (ABS)
Mark 1900	Organotin heat stabilizer available from Crompton
	Corporation, Middlebury, CT
G70S	Complex ester from Cognis Corp.
G16	Fatty acid ester of glycerine from Cognis Corp.
B866	Blendex 866 processing aid containing
	methylmathacrylate-acrylonitrile-styrene available
	from Crompton Corporation, Middlebury, CT

The compositions of Examples 1-20 and Comparative Example A were then evaluated in accordance with the following test methodologies as set forth in Table II:

TABLE II

Test Description

Izod D256-2002

Heat Distortion Temperature D648

Vicat D1525-96

Capillary D3835-2002

Haze and Transmittance D1003

The following Examples 1-20 and Comparative A are set forth in Table III. The amounts of components in the composition are given in parts by weight.

TABLE III


	Example	Example	Example	Example	Example	Example	Example	Example	Example	Example	Example
Component	1	2	3	4	5	6	7	8	9	10	11

PVC K60 (614)	40.00	50.00	30.00	25.00	25.00	25.00	41.67	25.00	30.42	29.17	40.00
PVC K66	15.00	0.00	5.00	15.00	0.00	15.00	6.67	0.00	16.67	6.67	0.00
(110 × 427)
HDT Modifier	35.00	35.00	40.00	50.00	50.00	35.00	39.17	60.00	40.42	51.67	50.00
B336	10.00	15.00	25.00	10.00	25.00	25.00	12.50	15.00	12.50	12.50	10.00
Mark 1900	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0
G70S	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0
G16	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0
B866	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0
Izod Impact	1.415	11.562	15.581	0.802	12.394	17.528	4.276	1.637	4.352	1.465	0.619
1/8 in.
Std. Dev.	0.138	0.150	0.307	0.066	0.262	0.320	0.172	0.060	0.125	0.229	0.061
HDT 66PSI	77	78	79	80	80	78	78	80	79	80	80
0.125 inch
(° C.)
HDT 264PSI	73	73	74	75	75	71	74	76	74	74	75
0.125 inch
(° C.)
Vicat	81	81	81	84	83	81	83	84	82	84	84
(° C.)
Opticals
0.125 inch
trans.	66.007	68.453	65.178	68.449	65.705	66.28	68.271	69.655	69.576	69.239	69.342
YI	31.074	32.254	39.601	29.904	38.651	38.85	31.253	32.56	29.406	30.498	29.791
Haze	31.763	27.696	30.487	30.582	30.488	30.488	26.762	25.383	26.535	25.822	25.457
Capillary
rheometer -
190 deg. C.,
0.040 orifice,
100-1000
1/sec
100	29468	29163	30643	26400	27170	32993	28651	23739	29557	25691	24926
500	9787	9741	9963	8962	9011	10553	9627	8153	9723	8779	8538
1000	5945	5950	6086	5553	5600	6382	5901	5126	5947	5487	5324

	Example	Example	Example	Example	Example	Example	Example	Example	Example	Comparative
Component	12	13	14	15	16	17	18	19	20	Example A

PVC K60 (614)	35.00	25.00	25.00	29.17	25.00	40.00	40.00	25.00	50.00	100.00
PVC K66	4.17	0.00	25.00	11.67	0.00	0.00	0.00	25.00	0.00	0.00
(110 × 427)
HDT Modifier	45.00	60.00	35.00	39.17	50.00	35.00	50.00	35.00	35.00	0.00
B336	15.83	15.00	15.00	20.00	25.00	25.00	10.00	15.00	15.00	12.00
Mark 1900	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0	2.0
G70S	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0
G16	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0
B866	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0	1.0
Izod Impact	8.104	1.686	12.435	15.732	12.516	16.484	0.595	12.408	11.081	23.977
1/8 in.
Std. Dev.	0.193	0.181	0.433	0.317	0.301	0.208	0.085	0.26	0.207	0.315
HDT 66PSI	79	81	78	78	80	78	80	78	78	73
0.125 inch
(° C.)
HDT 264PSI	75	76	74	74	75	74	76	73	73	70
0.125 inch
(° C.)
Vicat (° C.)	82	84	82	82	83	81	84	82	81	79
Opticals
0.125 inch
trans.	69.118	68.226	68.767	68.166	66.201	66.158	68.677	69.402	69.178	73.741
YI	32.044	34.097	31.812	35.075	38.496	39.104	29.01	30.81	31.628	24.75
Haze	26.612	26.335	27.295	27.88	30.289	29.761	27.58	27.685	27.385	30.353
Capillary
rheometer -
190 deg. C.,
0.040 orifice,
100-1000
1/sec
100	27638	23467	32039	30083	27321	30078	24449	32378	29073	39362
500	9228	7846	10348	9815	9069	9868	8436	10448	9681	12141
1000	5708	4956	6242	5991	5612	6016	5258	6307	5910	7191

The above results show the following advantages of the present invention as exemplified in Examples 1-20 as compared with Comparative Example A.
More particularly, Examples 1-20 show a higher heat distortion temperature. For example, at 264 PSI, all of the Examples possessed a heat distortion temperature ranging from 71° C. to 76° C. whereas Comparative Example A was at 70° C.
Moreover, the blend of the invention provides a composition having easier processing characteristics as demonstrated by the dramatically lower viscosities of the molten blends as compared to the Comparative Example A.
While the above description contains many specifics, these specifics should not be construed as limitations of the invention, but merely as exemplifications of preferred embodiments thereof. Those skilled in the art will envision many other embodiments within the scope and spirit of the invention as defined by the claims appended hereto.

Claims

1. A clear, impact modified, heat resistant polyvinyl halide composition comprising:

(a) at least one polyvinyl halide;

(b) at least one clear impact modifier possessing a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide; and

(c) at least one clear heat modifier comprising a terpolymer obtained by the copolymerization of a vinyl aromatic monomer, an acrylic nitrile monomer and an alkylacrylate or alkylmethacrylate, wherein the terpolymer possesses a refractive index which is not more than about 2% above or below the refractive index of the polyvinyl halide and possesses a weight average molecular weight ranging from about 75,000 to about 400,000;

wherein (a) comprises from about 20 to about 60 weight percent, (b) comprises from about 10 to about 25 weight percent and (c) comprises from about 25 to about 60 weight percent, based on the total weight of the combined weight of (a), (b) and (c).

2. The polyvinyl halide composition of claim 1, wherein the vinyl aromatic monomer is selected from the group consisting of styrene, alphamethylstyrene, halogenated styrene, vinyltoluene, alkoxystyrene and mixtures thereof.

3. The polyvinyl halide composition of claim 1, wherein the acrylic nitrile monomer is selected from the group consisting of methacrylonitrile, ethacrylonitrile, chloroacrylonitrile, acrylonitrile and mixtures thereof.

4. The polyvinyl halide composition of claim 1, wherein the alkyl acrylate or alkyl methacrylate is selected from a group consisting of methyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate and mixtures thereof.

5. The polyvinyl halide composition of claim 1, wherein the terpolymer possesses a weight average molecular weight from about 100,000 to about 200,000.

6. The polyvinyl halide composition of claim 1, wherein the polyvinyl halide is selected from the group consisting of vinyl halide homopolymers, vinyl halide copolymers and mixtures thereof.

7. The polyvinyl halide composition of claim 6, wherein the vinyl halide homopolymers are selected from the group consisting of polyvinyl chloride, polyinylidiene chloride, polyvinyl bromide, polyvinyl fluoride, polyvinylidene fluoride and mixtures thereof.

8. The polyvinyl halide composition of claim 6, wherein the vinyl halide copolymers are selected from the group consisting of vinylidene chloride, vinyl acetate vinyl butyrate, vinyl benzoate, diethyl fumarate, diethyl maleate, vinyl propionate, methyl acrylate, 2-ethyhexyl acrylate, butyl acrylate, ethyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, hydroxyethyl methacrylate, methyl α-chloracrylate, styrene, vinyl ethyl ether, vinyl chloroethyl ether, vinyl phenyl ether, vinyl methyl ketone, vinyl phenyl ketone, 1-fluoro-1-chloroethylene, acrylonitrile, chloroacrylonitrile, allylidene diacetate, chloroallylidene diacetate, ethylene, propylene and mixtures thereof.

9. The polyvinyl halide composition of claim 6, wherein the vinyl halide polymer blends are selected from the group consisting polyvinyl chloride and polyethylene, polyvinyl chloride and chlorinated polyethylene, polyvinyl chloride and polymethyl methacrylate, polyvinyl chloride and polybutylmethacrylate, polyvinyl chloride and polystyrene, polyvinyl chloride and acrylonitrile-butadiene-styrene copolymer, polyvinyl chloride and polyethylene and polymethyl methacrylate, and mixtures thereof.

10. The polyvinyl halide composition of claim 9, wherein the polymer blends comprise physical blends of at least two distinct polymeric species and contain from about 25 to about 95 weight percent vinyl halide homopolymer.

11. The polyvinyl halide composition of claim 1, wherein the impact modifier comprises a rubber modified with a thermoplastic resin.

12. The polyvinyl halide compositions of claim 11, wherein the impact modifiers are selected from a group consisting of ethylene-vinyl acetate copolymer, ethylene-propylene copolymer, polybutadiene-acrylonitrile-styrene copolymer, polybutadiene-styrene-methyl methacrylate, polybutylacrylate, crosslinked acrylic rubber, styrene-butadiene copolymer and acrylonitrile-butadiene copolymer.

13. The polyvinyl halide composition of claim 1, characterized in that the ⅛ inch Izod impact strength measured at a temperature of 23° C. is at least about 1.0 ftlb/in.

14. The polyvinyl halide composition of claim 1, wherein the impact modifier possesses a refractive index which is not more than about 1% above or below the refractive index of the polyvinyl halide.

15. The polyvinyl halide composition of claim 1, wherein the impact modifier possesses a refractive index which is not more than about 0.05% above or below the refractive index of the polyvinyl halide.

16. The polyvinyl halide composition of claim 1, wherein the terpolymer possesses a refractive index which is not more than about 1% above or below the refractive index of the polyvinyl halide.

17. The polyvinyl halide composition of claim 1, wherein the terpolymer possesses a refractive index which is not more than about 0.05% above or below the refractive index of the polyvinyl halide.